Literature DB >> 15118321

Novel lipoxygenase inhibitors, tetrapetalone B, C, and D from Streptomyces sp.

Toshikazu Komoda1, Madoka Kishi, Naoki Abe, Yasumasa Sugiyama, Akira Hirota.   

Abstract

Three novel lipoxygenase inhibitors, tetrapetalone B (2, C(28)H(35)NO(9)), C (3, C(26)H(34)NO(8)), and D (4, C(28)H(36)NO(10)), were isolated from a culture broth of Streptomyces sp. USF-4727 that produced a lipoxygenase inhibitor tetrapetalone A (1) simultaneously. Each chemical structure was revealed by spectroscopic evidence, this suggests that these three compounds are structurally related to 1. They had a tetracyclic skeleton and a beta-D-rhodinosyl moiety. Tetrapetalone B, C, and D inhibited soybean lipoxygenase with IC(50): 320, 360, and 340 microM respectively.

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Year:  2004        PMID: 15118321     DOI: 10.1271/bbb.68.903

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  6 in total

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4.  Studies toward the AB ring system of the tetrapetalone natural products.

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  6 in total

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